TVT Operations....How many of you have found this successful?

Posted , 62 users are following.

I had a TVT op five years ago, and had no idea of the problems some women had with this, until I read about them on here.

Could the women who have had this operation successfully please stop by and tell us how you are, and how long ago you had your TVT.

Thanks in advance.

2 likes, 197 replies

197 Replies

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  • Posted

    Just had my tvt operation last week Wednesday ..bit anxious now cos I'm reading negative thinges

    About it.. stI'll aynt fully mobile. How long can I not drive for they say up to 6 weeks but is that ok.

  • Posted

    I had the op over 12 yrs ago and it has literally ruined my life. Since the second I woke up from the anaesthetic I was in severe pain in my right groin and could barely move my right leg. I have scar tissue which together with the constant pain and difficulty moving my right leg has ruined my sex life. I can't exercise , struggle to walk or lift my right leg so I've put weight on and hate myself. I have developed fibromyalgia, don't know if it's connected but I'm now sensitive to loads of stuff. And it didn't even work. I'm told I need a new hip but I don't believe it and I'm positive it won't fix everything. I hate my life and wish I'd never had this vile surgery. I only needed it because I leaked after a hysterectomy 😕

    • Posted

      Where are you from Vicky? Can you get referred to one of the mesh complication specialists? I had mine in 12 years and after years of pain and stiffness I had it removed in Oxford. All that chronic leg pain has reduced massively and I can walk again. I also have fibromyalgia as so many women who have had this type of surgery. It's worth seeing if you can see someone who knows what they are talking about and maybe get it removed xx

    • Posted

      I had mine done some years I had to have part of my bladder removed due to complications they refused to remove all of the tape I am in constant pain and last pee sample showed pus cells worse thing i ever did in my life it can only get worse now I'm even contemplating having my bladder removed 

    • Posted

      That is horrific. I am so sorry for your suffering. This procedure can cause life changing complications. Women are still not being given the true picture before they decide to have it done or not. I am so so lucky that my issues were not like yours. I may have pain and stiffness but I still have all my internal organs intact. Much love to you xx
  • Posted

    I had Rectocele prolapse and Transvaginal Repair September 2016. After the pain relief wore off I was in excruciating pain in my lower back and my buttocks. On fire, stabbing etc I was then allergic to Morphine and the next pain relief they tried both with co-codemol which I was allergic to. After breaking two teeth with pain and 4 days with excruciating pain I was given an MRI with results telling me I had Chronic Nerve Damage. Ten days in hospital and given Gabapentin, Sublingual and Lydocaine Patches I came home. Cutting a long story short I was back in hospital before Christmas and again Friday. The pain is continuous and is ruining my life. I try to work but driving exasperates the pain. I have my GP tomorrow and I want and need answers. I believe the TVT is causing this. I have no life at present and am so sick of the pain. I had no pain like this before surgery, yet they now say Degenerative is the cause. If that were the case I'd have been on the medication before the surgery

    • Posted

      Hi, this whole issue is hot stuff at the mo as it was on tv last week on Victoria Derbyshire show. Don't met them fob you off. Have a look online at Sling the Mesh and If you or on Facebook join the Sling the mesh group. There are 1600 women in a similar place as you. You are not alone x

  • Posted

    Mine was a disaster to such an extent that I would like to see it banned my advice to anyone is dont do it 
  • Posted

    Hiya,

    I had this operation 15 years ago and haven't looked back. Best thing I did for my confidence.

  • Posted

    Hi I also had my TVT op in 2004. I thought it was wonderful not wetting myself when I sneezed or laughed, although my urge incontinence went worse immediately. I have suffered years of what I thought was thrush, and recurrent UTI's. I have been in pain and not felt well for years but over the last year it has become too painful to have sex, have recently bled and I feel that I am sat on something underneath but I can't see it in a mirror. I have been to my GP and asked to be referred to Dr Elneil to have it checked and removed. She has referred me back to the Consultant who did it! I am now incontinent of my bowel and bladder, have chronic pain everyday, and finding out about the Mesh problem has been a 'lightbulb' moment. I would have recommended it to anyone, as it did work for me, but now knowing that all of my health problems probably come from this makes me so angry and upset and I want it out! I am probably one of the earliest patients to have it done and it has ruined my life!

  • Posted

    I would like some advice I had tvt surgry last July nothing but problems in Jan I had to go in for surgery BC the tape went thru my vaginal wall . My dr said I should be good but now we are in May and I still have bad pain and my bladder problems are worse now I'm scheduled to have tvt tape removal on June 9 has anyone went thru that surgery and can tell me what I mite go thru thanks

    • Posted

      Hi Lisa. I had my TVT completely removed 10 weeks ago in Oxford. Please be very careful and make sure the surgeon knows how to remove as it is a high risk procedure and if not done by someone experienced can make things worse. Also make sure it is a full removal and not a partial as some surgeons will tell you it is full when it is absolutely not. Your body is only doing what it is supposed to by trying to push out a foreign body. Some women react more than others. If you are on Facebook please look at UK Sling the Mesh group for lots of advice from 2000 women in same boat as yourself
  • Posted

    I had this op ten year s ago, now having tests for bleeding and back pain
  • Posted

    Hi I had this op 9 years ago and I had a ventral roctopexy too...The TVT was done as I was advised the rectopexy couldmake my bladder worse than it was so had two surgeons working in tandam. I asked was it safe because I had researched about bladder weakness ops before and decided against them. I was assured it would be ok so went ahead with it. At first it was good I didn't need the pads but as time went by I found I wasn't as dry as I should have been so started to use pads again. I went back to the hospital to see the surgeon who did the op about three years ago, he refered me to physio for bladder training I even bought a bladder training machine to help none of this has been successful. I have for the past few years suffered terribly with joint pain mainly hip and leg and put it down to age. I was told it was osteoarthritis. But the last two years have been really awful, I asked for xrays and I was then told it was not osteoarthritis! I have been taken to A&E hospital on gas and air for low back pain on gas and air then given morphine on arrival then sent home with lignacain patches. I was told it was sciatica with no tests or investigations. I seen a rheumatologist who I told it was my large joints that were affected she scanned my fingers!! I have asked for stronger pain relief now I am refferred to a pain management clinic. I sit here now with terrible pain in my left groin, hips and leg I am now sleeping during the day too which is something I never did the pain is worse I cant walk very far without the pain getting stronger. When I pee it stops and starts I don't have the sensation I used to have in this area. Please can someone help, where do I go now? Thank you 

  • Posted

    Hi

    I had tvt sling and total hyst and cystocele recotocele and endocele repair done 17 months sgo. Tvt sling never worked. My doctor now recommends urethral bulking. Im very reluctant to get any more procedures done after not being told risks from tvt. Now also have pain with intercourse i didnt have previously. Went to pelvic physical therapy no improvement. Had second opinion and that dr suggested more pt with another therapist and the bulking. Also went on Mybetriq for several months and second opinion had me go off of it since it wasnt working. Ive had swelling of hands and feet since this surgery as well that i thought maybe side effect of mybetriq but im not taking it anymore. Surgeon put me on vagifem and sevond opinion put me on estrace cream instead. Dont feel eithet one has helped at all. I never expected to come out of surgery worse with more problems than i went in with. After my expierience i wouldnt recommend this surgery to anyone.

    • Posted

      cin0619 have a look at sling the mesh a group of women on fb its a wonderful helpful site I cried at the health issues these women have been given and also for myself too that we are not alone in this horrific situation. hope this helps best wishes x

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